At the international SCN8A Alliance, we believe firmly that every family - no matter their background, education, or medical experience - has the right to be able to understand the science of SCN8A and what is happening with their child. With this new series, SCN8A Unraveled, we are on a mission to help SCN8A families gain access to and better understand recent research and publications about SCN8A. With this information, families will be able to better raise awareness and
advocate for their children.
Developing an SCN8A ASO with Sophie Hill
SCN8A Genotype-Phenotype Correlations with Katrine Johannesen